1-(5-Bromo-2,4-difluoro-phenyl)-ethanone CAS 864773-64-8

Introduction:Basic information about 1-(5-Bromo-2,4-difluoro-phenyl)-ethanone CAS 864773-64-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

1-(5-Bromo-2,4-difluoro-phenyl)-ethanone Basic information

Product Name:1-(5-Bromo-2,4-difluoro-phenyl)-ethanone
Synonyms:1-(5-Bromo-2,4-difluoro-phenyl)-ethanone;5'-Bromo-2',4'-difluoroacetophenone 98%;1-(5-Bromo-2,4-difluorophenyl)ethan-1-one;5-broMo-2,4-difluoroacetophenobe;5'-Bromo-2',4'-difluoroacetophenone;Ethanone, 1-(5-bromo-2,4-difluorophenyl)-;1-(5-Bromo-2,4-difluorophenyl)
CAS:864773-64-8
MF:C8H5BrF2O
MW:235.03
EINECS:
Product Categories:
Mol File:864773-64-8.mol

1-(5-Bromo-2,4-difluoro-phenyl)-ethanone Chemical Properties

Boiling point 254.0±40.0 °C(Predicted)
density 1.614±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form crystalline solid
color White

Safety Information

HS Code 2914790090

1-(5-Bromo-2,4-difluoro-phenyl)-ethanone Usage And Synthesis

Uses1-(5-Bromo-2,4-difluoro-phenyl)-ethanone is a white powder crystal used in pharmaceutical synthesis and experimental research.
Synthesis

348-57-2

75-36-5

864773-64-8

1. in a dry reaction flask, anhydrous AlCl3 (1040 g, 7878.7 mmol) was added to 1-bromo-2,4-difluorobenzene (600 g, 3108.9 mmol) and stirred at 60 °C for 10 min.2. acetyl chloride (366 g, 4662.4 mmol) was added slowly dropwise to the above mixture, maintaining the temperature at 60 °C for 4 hours.3. after the dropwise addition was completed, the reaction mixture was continued to be stirred at 60 °C for 6 hours.4. the reaction mixture was cooled to -10 °C and ice (2450 g) was added slowly, this process was controlled to be completed within 1.5 hours.5. 12N HCl (1500mL) was added and stirred for 1 hour at room temperature.6. EtOAc (9000mL) was added for extraction, the organic layer was separated, washed with water, dried over anhydrous Na2SO4 and filtered.7. The organic phase was concentrated under pressure and the resulting residue was purified by silica gel column chromatography (eluent: petroleum ether/EtOAc, 50/1) to afford the target product 1-(5-bromo-2,4-difluorophenyl)ethanone (300 g, 41% yield).

References[1] Patent: WO2011/154374, 2011, A1. Location in patent: Page/Page column 26
[2] Patent: WO2012/62751, 2012, A1. Location in patent: Page/Page column 41-42
[3] Patent: US2013/252952, 2013, A1. Location in patent: Paragraph 0167; 0168
[4] Patent: US2004/220194, 2004, A1. Location in patent: Page 44; 45
[5] Patent: US2005/239795, 2005, A1. Location in patent: Page/Page column 36

1-(5-Bromo-2,4-difluoro-phenyl)-ethanone Preparation Products And Raw materials

Raw materials1,5-DIBROMO-2,4-DIFLUOROBENZENE-->N-Methoxy-N-methylacetamide-->Acetyl chloride-->1-Bromo-2,4-difluorobenzene
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